Clinical Research Associate (CRA) Training
Gain essential skills for a Clinical Research Associate role, covering informed consent, ICH-GCP guidelines, oncology protocols, source data verification, corrective actions, and inspection preparation. Perfect for clinical workers entering impactful research positions.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This focused Clinical Research Associate (CRA) Training builds hands-on skills for confident, rule-following trial monitoring. Learn ICH-GCP informed consent rules, key regulatory files, site file setup, drug tracking, protocol issues, source data checks and eCRF methods, serious adverse event management, CAPA creation, visit processes, and readiness for audits in cancer and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and IRB basics to conduct compliant trials swiftly.
- Monitor oncology studies by checking data, handling queries, and ensuring patient safety.
- Manage protocols and drug supplies by tracking deviations, dosing, and accountability.
- Oversee informed consent processes with version control, re-consent, and IRB updates.
- Create CAPA plans and reports to record issues, spot trends, and improve site performance.
Suggested summary
Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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